Phase V .Apa Seven
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PHASE 3
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Phase 3: Implementation
The third phase will elaborate the complete implementation plan that how the decided
methodology will be implemented to complete the research study. The topic of study includes nurses'
attitudes towards palliative patient care, and the use of euthanasia will be focused on and aligned with
the methodology. The details about the data collection, data analysis, data interpretation will be the
discussion. The budget planning and the timeline of the study will also be discussed.
Steps
Choosing Participants
The methodology starts with the sampling, and the implementation phase starts from here to
the data analysis. The researcher has studied the different theoretical approaches of sampling relevant
studies, so the participation selection shows the researcher's knowledge of the subject. The sampling
process should be chosen carefully because failure to choose inappropriate sampling will result in
unexpected results (Asai, 2019).
Different sampling approaches and techniques can be used in the research study, and the
researcher needs to choose one that fits the subject of the study. It may look simple and easy, but the
whole process is highly complex, and the researcher has to study a lot to know what participants will
be suitable for the research. The appropriate decision-making approach needs to be used in this
process.
Before the selection, the exclusion criteria need to be defined, and it is to take the nurses in
the study. The subject is relevant to the nurses, so only they will be part of the study, and it also has
to be seen that only the nurses involved in palliative care will be taken. They will have the experience
of dealing with patients with severe illness and voluntary or involuntary use of euthanasia. Moreover,
the nurses should know the difficulties and challenges of dealing with such patients.
There will be 60 participants in the study, 50 participants will be faculty nurses, and ten will
be in-charge nurses. The nurses will be aged above 25 years of age, and it will be seen that the
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selection should be based on research experiences. Moreover, the details of the study can be
disturbed if the coronavirus persists (Berghs, 2005).
Euthanasia is an essential concern in nursing, and it is given either voluntary or involuntary,
and the nurses have to take care of them. Palliative care is essential for the patients, and the nurses
involved in it will be taken in the research. The nurses have to be chosen based on their knowledge of
the subject. Palliative care is essential, and it will be researched in detail by the experience of nurses.
There are specific characteristics of nurses who will be selected for the study, and they should
know the challenges of voluntary and involuntary euthanasia. Euthanasia remains an arguable topic
because there are different ethical and moral standards are involved in its use. Moreover, the nurses
will be informed beforehand that their time will be taken for the interviews.
Coronavirus has affected all industries, and the healthcare industry has become highly
vulnerable. The hospitals have put high restrictions on the outsiders that they cannot visit without a
severe issue. The researchers usually plan to conduct the research and collect the data in live
interaction, but the situation might change. The coronavirus can alter the plan, and other ways will be
considered.
The priority will be to contact the nurses in the healthcare centers or the hospitals. Still, it
depends on the hospital administration and the nurses whether they will visit them or not. If physical
data collection is not possible, virtual meetings will be arranged.
The next step will be to contact the hospital management, and they will be informed of the
purpose of the research. The hospital management already knows the importance of using euthanasia
in the hospitals, and the nurses are required to use voluntary and involuntary euthanasia with the
patients. So, they will be asked to approve the 60 nurses and the whole duration of nurses.
Ethical Standards
A few ethical standards are essential for nursing, so they should be followed, and some of
them are discussed below.
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Consent
The research cannot be conducted without taking the consent of participants because it has
been seen that the research needs to be conducted for publishing purposes. If the participants are not
informed of the research purpose and the aim to collect the data, the circumstances will deteriorate.
So, the researcher needs to know why they are contacted and their role in the research. If they are
comfortable with the purpose of the research and their responsibilities, the nurses will then decide
whether they will be part of the research or not. All those who will agree will be contacted further for
the research (Cardiff University, 2014).
There is no possibility that a research project will only have advantages, but there are some
risks. It is part of ethical standards to inform the nurses about the side effects or risks of the research.
Moreover, it is seen that the researcher will have the duty to inform them the confidential information
about the research. The researcher does not disclose the facts about the research before time, but the
participants are necessary to be announced. If they are not told, the ethical standards will be violated,
and the research will lack the aspect of ethical considerations.
Confidentiality
After selecting participants, they are given assurance by the researcher that their privacy will
not be disturbed. Sometimes, the personal information is to be collected as well because the names,
contact numbers, and other details are necessary, so the participants are hesitant to give their details
because they are not sure whether they will use it for the research purpose only or if there will be any
other use. The nurses are the participants, and they are educated to understand the nature of research
easily. The research will give them the guarantee that there is no use of personal data. Everything will
be saved and will be wasted after the completion of the research. So, these factors should be kept in
mind during the research (Casterle, 2006).
Autonomy
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Autonomy is similar to the consent of participants, so the final stage will be to ask the
participants that they want to be a part of the research. If they're going to be part of it, a consent form
will be given to them, and they will sign it to ensure that they have decided on their own and have
given the surety that the researcher will keep the data safe private. So, they are agreed to be part of
the research (Ferrell, 2018).
Beneficence
All the professions have respect and dignity, and no one is allowed to mistreat it. For
example, if the nurses are taken as participants, they will be respected. There is no reason to harm
their privacy and respect. The hospital management and administration will be ensured that their staff
and nurses will be given high respect. Their dignity is essential for the researcher, and he will be
thankful to allow them to be a part of the research (Henson, 2016).
Data Analysis
The next step that helps to interrupt, describe and analyze the data is data analysis. The
statistical tools are used to know the probability of the relationship and prediction of the relationship
between the variables. The research will be a mixed methodology, including both the qualitative and
quantitative approaches. So, it will be in consideration to know the appropriate statistical techniques.
The basic and descriptive statistics will be used for data analysis (Wright, 2016).
Training
The research outcomes will decide the shortcomings in palliative care, and nurses will be
given guidelines on how they should deal with the patients and the gaps that need to be addressed
(Weaver, 2018).
Timeline
Table 1
Gantt Chart
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Week 1 2 3 4 5 6 7 8
Choosing Participants
Moral and Ethical protocols training
Data gathering process
Data Analysis
Training of nurses
Final report submission
Budget
It is the most important section of the report because it includes the expenditure and costs of
different activities involved in the research. The table shows the details of costs and budget.
Table 2
Budget
Item Cost ($)
Promotion 600
Training for ethical standards 1300
Survey costs 1200
Result analysis 1700
Training for nurses 12000
Total 16,800
References
Asai, A., Ohnishi, M., Nagata, S. K., Tanida, N., & Yamazaki, Y. (2019). Doctors' and nurses'
Attitudes towards and experiences of voluntary euthanasia: a survey of members of the
Japanese Association of Palliative Medicine. Journal of medical ethics, 27(5), 324-330.
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Berghs, M., De Casterle, B. D., & Gastmans, C. (2005). The complexity of nurses’ attitudes toward
euthanasia: a review of the literature. Journal of Medical Ethics, 31(8), 441-446.
Cardiff University. (2014). Palliative Medicine for Health Care Professionals
(MSc)https://www.cardiff.ac.uk/study/postgraduate/taught/courses/course/palliative-
medicine-for-health-care-professionals-MSc-part-time. Cardiff University. Retrieved
26 September 2021, from
https://www.cardiff.ac.uk/study/postgraduate/taught/courses/course/palliative-medicine-
for-health-care-professionals-MSc-part-time.
Dierckx de Casterle, B. (2006). Nurses' views on their involvement in euthanasia: a qualitative
study in Flanders (Belgium). Journal Of Medical Ethics, 32(4), 187-192.
https://doi.org/10.1136/jme.2005.011783
Ferrell, B. R., Twaddle, M. L., Melnick, A., & Meier, D. E. (2018). National consensus project
clinical practice guidelines for quality palliative care guidelines. Journal of palliative
medicine, 21(12), 1684-1689.
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Henson, L. A., Gomes, B., Koffman, J., Daveson, B. A., Higginson, I. J., & Gao, W. (2016).
Factors associated with the aggressive end of life cancer care. Supportive Care in
Cancer, 24(3), 1079-1089.
Weaver, M. S., Wichman, B., Bace, S., Schroeder, D., Vail, C., Wichman, C., & Macfadyen,
A. (2018). Measuring the impact of the home health nursing shortage on family
caregivers of children receiving palliative care. Journal of Hospice and Palliative
Nursing, 20(3), 260.
Wright, A. A., Keating, N. L., Ayanian, J. Z., Chrischilles, E. A., Kahn, K. L., Ritchie, C. S., ...
& Landrum, M. B. (2016). Family perspectives on aggressive cancer care near the end of
life. Jama, 315(3), 284-292.
- PHASE 3
- Phase 3: Implementation
- Steps
- Budget